86232-91-9

Basic information

• Product Name: 1H-1,5-Benzodiazepine, 2-(4-chlorophenyl)-2,3-dihydro-4-phenyl-
• CAS NO: 86232-91-9
• Molecular Formula: C21H17ClN2
• Molecular Weight: 332.832
• Mol File: 86232-91-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1H-1,5-Benzodiazepine, 2-(4-chlorophenyl)-2,3-dihydro-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,5-Benzodiazepine, 2-(4-chlorophenyl)-2,3-dihydro-4-phenyl-(86232-91-9)
• EPA Substance Registry System: 1H-1,5-Benzodiazepine, 2-(4-chlorophenyl)-2,3-dihydro-4-phenyl-(86232-91-9)

Safety Data

• Hazardous Substances Data: 86232-91-9(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 104-88-1 4-chlorobenzaldehyde 
• 24721-26-4 4-chlorochalcone 
• 95-54-5 1,2-diamino-benzene 
• 956-04-7 3-(4-chlorophenyl)-1-phenylprop-2-en-1-one 
• 88-74-4 2-nitro-aniline 

Downstream Products

• 716-79-0 2-phenyl-1H-benzoimidazole 
• 1019-85-8 2-(4-chlorophenyl)benzimidazole 

Relevant articles and documents

Graphite oxide: A metal free highly efficient carbocatalyst for the synthesis of 1,5-benzodiazepines under room temperature and solvent free heating conditions

Graphite Oxide (GO), an attractive metal free carbocatalyst, was employed as a green and highly efficient catalytic system for the synthesis of 1,5-benzodiazepines. The reaction was studied at room temperature as well as at 80°C under solvent free heating

SbCl3-Al2O3-catalyzed, solvent-free, one-pot synthesis of benzo[b]1,4-diazepines

This article explores the use of antimony(III) chloride adsorbed on neutral alumina as an efficient catalyst for the one-pot synthesis of benzo[b]1,4-diazepines (83-94%) under solvent-free conditions. The process is easy, efficient, ecofriendly, and econo

A new and efficient one-pot solid-supported synthesis of 1,2,4,6-tetraaryl-1,4-dihydropyridines

1,2,4,6-Tetraaryl-1,4-dihydropyridines were obtained by the one-pot reaction of chalcones and substituted anilines on the surface of Bi(III)nitrate-Al2O3. The reaction seems to proceed via β-oxygenation of Bi(III) enolised chalcones followed by Michael addition and heteroannulation with simultaneous retro aldol disproportionation. The presence of the ring-activating groups at ortho and para positions in the aniline seems to be essential for the reaction.